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Oxygen adsorption reaction

In addition to effects on the concentration of anions, the redox potential can affect the oxidation state and solubility of the metal ion directly. The most important examples of this are the dissolution of iron and manganese under reducing conditions. The oxidized forms of these elements (Fe(III) and Mn(IV)) form very insoluble oxides and hydroxides, while the reduced forms (Fe(II) and Mn(II)) are orders of magnitude more soluble (in the absence of S( — II)). The oxidation or reduction of the metals, which can occur fairly rapidly at oxic-anoxic interfaces, has an important "domino" effect on the distribution of many other metals in the system due to the importance of iron and manganese oxides in adsorption reactions. In an interesting example of this, it has been suggested that arsenate accumulates in the upper, oxidized layers of some sediments by diffusion of As(III), Fe(II), and Mn(II) from the deeper, reduced zones. In the aerobic zone, the cations are oxidized by oxygen, and precipitate. The solids can then oxidize, as As(III) to As(V), which is subsequently immobilized by sorption onto other Fe or Mn oxyhydroxide particles (Takamatsu et al, 1985). [Pg.390]

Methane reforming with carbon dioxide proceeds in a complex sequence of reaction steps involving the dissociative adsorption/reaction of methane and COj at metal sites. Hydrogen is generated during methane dissociation In the second set of reactions CO2 dissociates into CO and adsorbed oxygen. The reaction between the surface bound carbon (from methane dissociation) and the adsorbed oxygen (from CO2 dissociation ) yields carbon monoxide. A stable catalyst can only be achieved if the two sets of reactions are balanced. [Pg.471]

Bhzanac BB, Lucas CA, Gallagher ME, Arenz M, Ross PN, Markovic NM. 2004a. Anion adsorption, CO oxidation, and oxygen reduction reaction on a Au(lOO) surface The pH effect. J Phys Chem B 108 625-634. [Pg.199]

Wang YX, Balbuena PB. 2005b. Potential energy surface profile of the oxygen reduction reaction on a Pt cluster Adsorption and decomposition of OOH and H2O2. J Chem Theory Comput 1 935-943. [Pg.314]

Thus, the model proposed explains the effect of CO on electric conductivity of several oxides only in case when oxygen is present in ambient volume which was observed in numerous experiments. Accordingly, the fact of existence of relatively narrow temperature interval in which an adsorbent is sensitive to CO becomes clear. This can be linked with the fact that if the operational temperature To is small the reaction products (in case of CO this is CO2) cannot get desorbed (see expression (2.80)), i.e. regeneration of the centers of oxygen adsorption is not feasible. If Tq is very high both adsorption of oxygen and reducing gas should be ruled out. [Pg.145]

Kds are the constants of rates of chemical reactions of oxygen adsorption and desorbtion from ZnO film and Aq are electron work function from ZnO before oxygen gets adsorbed and its variation caused by dipole moment of adsorbed complexes being formed U is the adsorption activation energy of non-electrostatic nature [ M] is the concentration of solvent molecules. Apparently we can write down the following expression for the stationary system ... [Pg.211]

These levels of interfacial redox electrons are connected with the hydrogen and oxygen electrode reactions. As noted in Sec. 5.1.2, the electron level of adsorbate particles is broadened by contact adsorption and undergoes the Franck-Condon level splitting due to a difference in adsorption energy between the oxidized particle and the reduced particle on the interface of semiconductor electrodes as shown in Fig. 5-59. [Pg.190]

As the adsorption affinity of redox particles on the electrode interface increases, the hydrated redox particles is adsorbed in the dehydrated state (chemical adsorption, contact adsorption) rather than in the hydrated state (ph3 ical adsorption) as shown in Fig. 7-2 (b). Typical reactions of redox electron transfer of dehydrated and adsorbed redox particles on electrodes are the hydrogen and the oxygen electrode reactions in Eqns. 7-6 and 7-7 ... [Pg.215]

Adsorption inhibitors act by forming a film on the metal surface. The action of traditional oil-based red lead paint formulations presumably involves the formation of soaps and the precipitation of complex ferric salts that reinforce the oxide film. There has been substantial interest in recent years in development of replacements for lead-based and chromate-based inhibitor systems. Adsorption inhibitors based on pol3rmers have been of particular interest. In this volume, Johnson et al. and Eng and Ishida discuss inhibitors for copper 2-undecylimidazole is shown to be effective in acid media, where it suppresses the oxygen reduction reaction almost completely. Polyvlnyllmidazoles are shown to be effective oxidation inhibitors for copper at elevated temperatures. Also in this volume, Chen discusses the use of N-(hydroxyalkyl)acrylamide copolymers in conjunction with phosphate-orthophosphate inhibitor systems for cooling systems. [Pg.5]


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See also in sourсe #XX -- [ Pg.8 , Pg.283 , Pg.305 , Pg.323 ]




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Oxygen adsorption

Oxygen electroreduction reaction hydrogen adsorption

Oxygen reduction reaction acid adsorption

Oxygen reduction reaction intermediates adsorption

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